Evidence map›Paper›PMID 41479917›Full record

ReviewFrontiers in immunology2025

Research progress on recombinant NDV in cancer therapy.

Jiating Sun, Jia Wang, Min Xiao, Liming Chen, Yi Guan

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jiating SunGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Shantou, Guangdong, China.
Jia WangGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Shantou, Guangdong, China.
Min XiaoGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Shantou, Guangdong, China.
Liming ChenGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Shantou, Guangdong, China.
Yi GuanGuangdong-Hong Kong Joint Laboratory of Emerging Infectious Diseases, Joint Institute of Virology (STU/HKU), Shantou University, Shantou, Guangdong, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Newcastle disease virus (NDV) has emerged as a promising oncolytic agent in cancer therapy. NDV not only directly lyses tumor cells but also activates the host's innate and adaptive immune responses, demonstrating potent antitumor activity. However, the efficacy of wild-type NDV is often limited and inconsistent. Advances in genetic engineering have led to the development of a new generation of highly effective and safe recombinant Newcastle disease viruses (rNDVs) by deleting non-essential viral genes or incorporating exogenous functional genes. These genetically engineered NDVs further enhance antitumor activity and optimize the tumor microenvironment by increasing pro-inflammatory cytokine secretion and inducing systemic antitumor immunity. In this review, we summarize the current status of rNDVs, modification strategies, antitumor mechanisms, clinical applications, and combination therapies involving rNDVs. We also discuss the current challenges in utilizing NDV for cancer therapy, including determining the most effective delivery routes, developing strategies to evade neutralizing antibodies, overcoming tumor heterogeneity, and identifying relevant biomarkers.

Indexed as

NeoplasmsNewcastle disease virusOncolytic VirotherapyOncolytic VirusesAnimalsGenetic EngineeringHumansTumor Microenvironmentcancer treatmentgene editingimmunotherapyNewcastle disease virusoncolytic virotherapy

Identifiers

PMID41479917
PMCPMC12753920

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.